Showing results (111-120 of 118) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 118 results.
Human Genetics|July 1, 1988
Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomesU Tantravahi, G D Stewart, M Van Keuren, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patientsA Moncla, P Malzac, M A Voelckel, et al.
Cytogenetics and Cell Genetics|January 1, 1982
Cytogenetic and flow cytometric studies of cells from patients with Fanconi's anemiaS A Latt, T N Kaiser, A Lojewski, et al.
American Journal of Human Genetics|April 1, 1995
The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2G A Silverman, S S Schneider, H F Massa, et al.
American Journal of Mental Deficiency|March 1, 1984
Molecular genetic approaches to human diseases involving mental retardationS A Latt, D M Kurnit, G P Bruns, et al.
Nature|July 29, 1993
A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locusY Nakatsu, R F Tyndale, T M DeLorey, et al.
Nature Genetics|November 14, 1997
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal regionP Jay, C Rougeulle, A Massacrier, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
Pageof 12